Gene: [14q11/ANG] angiogenin (phospholipase C activator; ribonuclease?); — Gene: [16p1313/GSPT1] G1 to S phase transition 1;


  • Gene: [14q11/ANG] angiogenin (phospholipase C activator; ribonuclease?);
  • Gene: [14q11/NRL] neural retina leucine zipper; [D14S46E ]
  • Gene: [14q112/CEBPE] CCAAT/enhancer binding protein (C/EBP), epsilon; [CRP1 ]
  • Gene: [14q112/CMA1] chymase 1, mast cell (chymase, heart; MIM:118938);
  • Gene: [14q112/CTLA1] cytotoxic T-lymphocyte-associated serine esterase 1 (CSP-B); granzyme B (cathepsin G-like enzyme 1); T cell/natural killer cells serine esterase 1;
  • Gene: [14q112/CTSGL2] cathepsin G-like 2 (protein h-CCPX); granzyme H (cytotoxic T-lymphocyte proteinase);
  • Gene: [14q112/CTSG] cathepsin G;
  • Gene: [14q112/NP] nucleoside phosphorylase (purine-nucleoside phosphorylase); T cell immunodeficiency (hyperinosinicuria);
  • Gene: [14q112/OXA1L] oxidase (cytochrome c) assembly 1-like protein;
  • Gene: [14q112/PSMB5] proteasome (prosome, macropain) subunit, beta type, 5 (homolog of yeast PRE2); multicatalytic endopeptidase complex epsilon chain (proteasome subunit X);
  • Gene: [14q112/PSME1] proteasome (prosome, macropain) activator subunit 1 (PA28 alpha); interferon, gamma-inducible protein 5111 (activator of multicatalytic protease, 29kD); [IFI5111 IFNI5 ]
  • Gene: [14q112/PSME2] proteasome (prosome, macropain) activator subunit 2 (PA28 beta);
  • Gene: [14q112/RABGGTA] Rab geranylgeranyl transferase, alpha subunit;
  • Gene: [14q112/TCL4] T cell lymphoma 4 associated breakpoint;
  • Gene: [14q112/TCR1AC] T cell receptor, Ti-alpha subunit, CON-region; [TCRA ]
  • Gene: [14q112/TCR1ADY] T cell receptor, Ti-alpha subunit, DIV-segment; [TCRA ]
  • Gene: [14q112/TCR1AJ] T cell receptor, Ti-alpha subunit, J-segment; [TCRA ]
  • Gene: [14q112/TCR1AV] T cell receptor, Ti-alpha subunit, VAR-region; [TCRA ]
  • Gene: [14q112/TCR1DC] T cell receptor, Ti-delta subunit, CON-region; [TCRD ]
  • Gene: [14q112/TCR1DJ1] T cell receptor, Ti-delta subunit, J1-segment; [TCRD ]
  • Gene: [14q112/TCR1DJ2] T cell receptor, Ti-delta subunit, J2-segment;
  • Gene: [14q112/TCRAV17] T-cell receptor, alpha variable region 17, segment 1; [TCRAV17S1 ]
  • Gene: [14q112/TCRAV5] T-cell receptor, alpha variable region 5, segment 1; [TCRAV5S1 ]
  • Gene: [14q112/TGM1] transglutaminase 1 (K polypeptide epidermal type I); protein-glutamine-gamma-glutamyltransferase (transglutaminase 1); ichthyosis congenita II, non-erythromatous lamellar ichthyosis (MIM:242300); ichthyosiform erythroder
  • Gene: [14q112/TRL1] tRNA leucine (anticodon AAG) 1;
  • Gene: [14q112/TRP1] tRNA proline (anticodon AGG) 1; [TRNP1 ]
  • Gene: [14q112/TRP2] tRNA proline (anticodon AGG) 2; [TRNP2 ]
  • Gene: [14q112/TRT2] tRNA threonine (anticodon UGU) 2;
  • Gene: [14q12/FKHL4] forkhead (Drosophila)-like 4;
  • Gene: [14q13/FKHL1] forkhead (Drosophila)-like 1 (brain factor 1; retroviral oncogene qin homolog); [QIN BF1 ]
  • Gene: [14q13/FKHL2] forkhead (Drosophila)-like 2 (brain factor 2; retroviral oncogene qin homolog); [BF2 ]
  • Gene: [14q13/NFKBIA] nuclear factor of kappa light chain gene enhancer in B-cells inhibitor, alpha; transcription factor kappa-B, inhibitor, alpha; [NFKBI IKBA ]
  • Gene: [14q13/PSMA6] proteasome (prosome, macropain) subunit, alpha type, 6 (homolog of yeast PRS2); multicatalytic endopeptidase complex iota chain (27kD prosomal protein);
  • Gene: [14q13/SSTR1] somatostatin receptor 1;
  • Gene: [14q13/TITF1] thyroid transcription factor 1; NK homeobox (Drosophila), family 2, A; [NKX2A TTF-1 ]
  • Gene: [14q13/TMIP] tetramelic mirror-image polydactyly (Laurin-Sandrow syndrome);
  • Gene: [14q2/ARVD1] arrhythmogenic right ventricular dysplasia 1; [ARVD ]
  • Gene: [14q2/BMP4] bone morphogenetic protein 4; [BMP2B ]
  • Gene: [14q2/BRF1] butyrate response factor 1 (EGF-response factor 1); [ERF1 TIS11B ]
  • Gene: [14q2/CRG] CHARGE association (coloboma, heart anomaly, choanal atresia, retardation, genital and ear anomalies);
  • Gene: [14q2/FNTB] farnesyltransferase, CAAX box, beta;
  • Gene: [14q2/HIF1A] hypoxia-inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor); [MOP1 ]
  • Gene: [14q2/HNRPI] heterogeneous nuclear ribonucleoprotein I (59.6kD); RNP particle, heterogeneous nuclear, I protein; polypyrimidine tract binding protein; [PTB ]
  • Gene: [14q2/LGALS3] lectin, galactoside-binding, soluble, 3; galectin 3 (35kD); [MAC2 ]
  • Gene: [14q2/OTX2] orthodenticle (Drosophila) homolog 2; homeobox protein OTX2;
  • Gene: [14q2/PGF] placenta growth factor, VPF/VEGF-related protein;
  • Gene: [14q2/RAD51L1] RAD51 (S. cerevisiae)-like 1; RAD51 (S. cerevisiae) homolog B; [RAD51B REC2 ]
  • Gene: [14q2/RTN1] reticulon 1; neuroendocrine-specific protein; [NSP ]
  • Gene: [14q2/ZNF46] zinc finger protein 46 (KUP); [KUP ]
  • Gene: [14q21/MGAT2] mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase; carbohydrate-deficient glycoprotein syndrome, type II (MIM:212066);
  • Gene: [14q21/MJD] Machado-Joseph disease; spinocerebellar ataxia 3 (olivopontocerebellar ataxia 3); [SCA3 ]
  • Gene: [14q21/PYGL] phosphorylase, glycogen; liver; glycogen storage disease, type VI (Hers disease);
  • Gene: [14q21/SOS2] son of sevenless (Drosophila) homolog 2;
  • Gene: [14q22/CDKN3] cyclin-dependent kinase inhibitor 3 (CDK2-associated dual specificity phosphatase); cyclin-dependent kinase interactor 1;
  • Gene: [14q22/GCH1] GTP cyclohydrolase 1; dystonia, dopa-responsive (MIM:128230); progressive, with diurnal variation (Segawa syndrome; MIM:128230); phenylketonuria, atypical severe (due to GTP cyclohydrolase 1 deficiency; MIM:233910);
  • Gene: [14q22/HSPA2] heat shock 70kD protein 2; [BIP2 ]
  • Gene: [14q221/KTN1] kinectin 1 (kinesin receptor); CG-1 antigen (leukocyte antigen) (MIM:600381); [CG1 ]
  • Gene: [14q23/FRA14B] fragile site 14q23, aphidicolin type, common;
  • Gene: [14q23/FUT8] fucosyltransferase 8 (alpha (1,6) fucosyltransferase);
  • Gene: [14q23/MAX] MAX protein (MYC associated factor X);
  • Gene: [14q23/MNAT1] menage a trois 1 (CDK-activating kinase assembly factor p35); [MAT1 p35 ]
  • Gene: [14q23/PSMA3] proteasome (prosome, macropain) subunit, alpha type, 3 (homolog of yeast PRS1); multicatalytic endopeptidase complex subunit C8;
  • Gene: [14q24/ACTN1] actinin, alpha 1; [AA1 ]
  • Gene: [14q24/CD39L4] CD39-like 4;
  • Gene: [14q24/DLST] dihydrolipoamide S-succinyltransferase (E2 component of 2-oxo-glutarate complex);
  • Gene: [14q24/LTBP2] latent transforming growth factor beta binding protein 2; Marfan syndrome, atypical; [LTBP-2 ]
  • Gene: [14q24/MDG1] microvascular endothelial differentiation gene 1;
  • Gene: [14q24/MTHFD] methylenetetrahydrofolate dehydrogenase (EC:1.5.1.5); methenyltetrahydrofolate cyclohydrolase (EC:3.5.4.9); formyltetrahydrofolate synthetase (EC:6.3.4.3);
  • Gene: [14q24/PXMP1L] peroxisomal membrane protein 1-like; [P70R PMP69 ]
  • Gene: [14q24/SFRS5] splicing factor, arginine/serine-rich 5 (p40); [SRp40 HRS ]
  • Gene: [14q24/SPTB] spectrin, beta, erythrocytic; spherocytosis 1; [SPH1 ]
  • Gene: [14q24/TGFB3] transforming growth factor, beta 3;
  • Gene: [14q241/FRA14C] fragile site 14q24.1, aphidicolin type, common;
  • Gene: [14q241/GPX2] glutathione peroxidase 2 (gastrointestinal);
  • Gene: [14q243/CHX10] homeobox 10 (C elegans ceh-10 homeo domain-containing homolog);
  • Gene: [14q243/EIF2B2] eukaryotic translation initiation factor 2B, subunit 2 (beta, 39kD);
  • Gene: [14q243/ESRRB] estrogen-related receptor beta; estrogen receptor-like 2; [ESRL2 ERR2 ]
  • Gene: [14q243/FOS] murine FBJ osteosarcoma viral homolog;
  • Gene: [14q243/PSEN1] presenilin 1; Alzheimer disease 3 (early onset); [AD3 PS1 ]
  • Gene: [14q243/RAP1AP] RAP1A, member of RAS oncogene family (K-rev) pseudogene; [KREV1P ]
  • Gene: [14q243/UBE2L1] ubiquitin-conjugating enzyme E2L 1;
  • Gene: [14q3/CYB5P3] cytochrome b-5 pseudogene 3;
  • Gene: [14q3/PI4] protease inhibitor 4 (kallistatin; kallikrein inhibitor); [KLST ]
  • Gene: [14q31/GALC] galactosylceramidase (galactocerebrosidase); leukodystrophy, globoid cell (Krabbe disease);
  • Gene: [14q31/OGR1] G protein-coupled receptor, ovarian cancer, 1;
  • Gene: [14q31/TSHR] thyroid stimulating hormone receptor (thyrotropin receptor); TSH resistance (unresponsiveness to thyrotropin);
  • Gene: [14q32/BDKRB1] bradykinin receptor B1 (G protein-coupled receptor);
  • Gene: [14q32/BDKRB2] bradykinin receptor B2 (G protein-coupled receptor);
  • Gene: [14q32/CALM1] calmodulin 1 (phosphorylase kinase, delta);
  • Gene: [14q32/CHGA] chromogranin A, parathyroid secretory protein 1; pancreastatin; chromostatin;
  • Gene: [14q32/ELK2] oncogene ELK2, member of ETS oncogene family;
  • Gene: [14q32/EMAP] echinoderm microtubule-associated protein-like protein; [EMAPL ]
  • Gene: [14q32/IFNI27] interferon, alpha-inducible protein 27; [IFI27 ]
  • Gene: [14q32/JAG2] jagged 2;
  • Gene: [14q32/TNFAI2] tumor necrosis factor, alpha-induced protein 2; [TNFAIP2 B94 ]
  • Gene: [14q32/USH1A] Usher syndrome 1A (autosomal recessive, severe; retinitis/deafness); [USH1 US1 ]
  • Gene: [14q32/VRK1] vaccinia related kinase 1 (vaccinia virus B1 related);
  • Gene: [14q321/AACT] alpha-1-antichymotrypsin;
  • Gene: [14q321/CBG] corticosteroid binding globulin; transcortin deficiency;
  • Gene: [14q321/GSC] goosecoid homeobox gene;
  • Gene: [14q321/PCI] protein C inhibitor; plasminogen activator inhibitor, type III; [PLANH3 PLGAI3 ]
  • Gene: [14q321/PI1] protease inhibitor 1 (anti-elastase), alpha-1-antitrypsin; alpha-1-antitrypsin deficiency, autosomal recessive; emphysema (liability?; chronic obstructive lung disease); hepatocellular carcinoma/cirrhosis (liability?); [P
  • Gene: [14q321/PIL] protease inhibitor 1 (alpha-1-antitrypsin)-like; alpha-1-antitrypsin-related protein (ATR); [ATR ARGS ]
  • Gene: [14q321/PRSC1] protease, cysteine, 1 (legumain);
  • Gene: [14q321/TCL1] T-cell leukemia 1, 14 kDa protein; T cell lymphoma 1 associated breakpoint;
  • Gene: [14q323/BST1] bone marrow stromal cell antigen 1;
  • Gene: [14q323/CKBE] creatine kinase, brain form, ectopic expression of;
  • Gene: [14q323/CKB] creatine kinase, brain form;
  • Gene: [14q323/CRIP2] cysteine-rich protein 2 (LIM domain protein ESP1);
  • Gene: [14q323/D14S1] DNA segment, single copy, probe p1; arbitrary restriction polymorphism-1; [RFLP14A ]
  • Gene: [14q323/DNCL] dynein, cytoplasmic-like; situs inversus viscerum? (MIM:270100); [DNECL ]
  • Gene: [14q323/HSPCAL4] heat shock 90kD protein, alpha-like 4;
  • Gene: [14q323/KNS2A] kinesin 2, light chain, member A (60-70kD); [KNS2 KLC1 ]
  • Gene: [14q323/MARK3] MAP/microtubule affinity-regulating kinase 3 (110kD); serine/threonine kinase MARK3; serine/threonine kinase p78;
  • Gene: [14q323/XRCC3] X-ray repair complementing defective repair in Chinese hamster cells 3;
  • Gene: [14q3233/AKT1] murine thymoma viral cell homolog 1; serine/threonine kinase, Rac-alpha;
  • Gene: [14q3233/IGHA1] immunoglobulin, heavy alpha-1 constant region;
  • Gene: [14q3233/IGHA2] immunoglobulin, heavy alpha-2 constant region (a2m marker);
  • Gene: [14q3233/IGHDYA10] immunoglobulin heavy chain, diversity region A10;
  • Gene: [14q3233/IGHDYA1] immunoglobulin heavy chain, diversity region A1; [IGD1 ]
  • Gene: [14q3233/IGHDYA2] immunoglobulin heavy chain, diversity region A2;
  • Gene: [14q3233/IGHDYA3] immunoglobulin heavy chain, diversity region A3;
  • Gene: [14q3233/IGHDYA4] immunoglobulin heavy chain, diversity region A4;
  • Gene: [14q3233/IGHDYA5] immunoglobulin heavy chain, diversity region A5; [DHQ52 ]
  • Gene: [14q3233/IGHDYA6] immunoglobulin heavy chain, diversity region A6;
  • Gene: [14q3233/IGHDYA7] immunoglobulin heavy chain, diversity region A7;
  • Gene: [14q3233/IGHDYA8] immunoglobulin heavy chain, diversity region A8;
  • Gene: [14q3233/IGHDYA9] immunoglobulin heavy chain, diversity region A9;
  • Gene: [14q3233/IGHDYB1] immunoglobulin heavy chain, diversity region B1;
  • Gene: [14q3233/IGHDYB2] immunoglobulin heavy chain, diversity region B2;
  • Gene: [14q3233/IGHD] immunoglobulin, heavy delta constant region;
  • Gene: [14q3233/IGHEP1] immunoglobulin, heavy epsilon constant region, pseudogene 1; [IGEP1 ]
  • Gene: [14q3233/IGHE] immunoglobulin, heavy epsilon constant region;
  • Gene: [14q3233/IGHG1] immunoglobulin, heavy gamma-1 constant region (Gm marker);
  • Gene: [14q3233/IGHG2] immunoglobulin, heavy gamma-2 constant region (Gm marker); IgG2 deficiency, selective;
  • Gene: [14q3233/IGHG3] immunoglobulin, heavy gamma-3 constant region (Gm marker);
  • Gene: [14q3233/IGHG4] immunoglobulin, heavy gamma-4 constant region (Gm marker);
  • Gene: [14q3233/IGHGP] immunoglobulin, heavy gamma constant region, pseudogene 1;
  • Gene: [14q3233/IGHJ1] immunoglobulin heavy chain, joining segment 1; [IGHJ ]
  • Gene: [14q3233/IGHJ2] immunoglobulin heavy chain, joining segment 2;
  • Gene: [14q3233/IGHJ3] immunoglobulin heavy chain, joining segment 3;
  • Gene: [14q3233/IGHJ4] immunoglobulin heavy chain, joining segment 4;
  • Gene: [14q3233/IGHJ5] immunoglobulin heavy chain, joining segment 5;
  • Gene: [14q3233/IGHJ6] immunoglobulin heavy chain, joining segment 6;
  • Gene: [14q3233/IGHJP1] immunoglobulin heavy chain, joining pseudogene 1;
  • Gene: [14q3233/IGHJP2] immunoglobulin heavy chain, joining pseudogene 2;
  • Gene: [14q3233/IGHJP3] immunoglobulin heavy chain, joining pseudogene 3;
  • Gene: [14q3233/IGHMAS] immunoglobulin, heavy mu-alpha switch region;
  • Gene: [14q3233/IGHM] immunoglobulin, heavy mu constant region;
  • Gene: [14q3233/IGHVA1] immunoglobulin heavy chain, var-region, class I, pep-1;
  • Gene: [14q3233/IGHVB1] immunoglobulin heavy chain, var-region, class II, pep-1;
  • Gene: [14q3233/IGHVC1] immunoglobulin heavy chain, var-region, class III, pep-1;
  • Gene: [14q3233/IGHVD1] immunoglobulin heavy chain, var-region, class IV, pep-1;
  • Gene: [14q3233/IGHVE1] immunoglobulin heavy chain, var-region, class V, pep-1;
  • Gene: [14q3233/IGHVE2] immunoglobulin heavy chain, var-region, class V, pep-2;
  • Gene: [14q3233/IGHVE3] immunoglobulin heavy chain, var-region, class V, pep-3;
  • Gene: [14q3233/IGHVF1] immunoglobulin heavy chain, var-region, class VI, pep-1;
  • Gene: [14q3233/IGHVP1] immunoglobulin heavy chain, var-region, pseudogene 1;
  • Gene: [14^/ADCY4] adenylate cyclase 4;
  • Gene: [14^/ATP5CL2] ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide-like 2;
  • Gene: [14^/CFL2] cofilin 2 (muscle);
  • Gene: [14^/COILP] coilin, p80 pseudogene;
  • Gene: [14^/COX7A3] cytochrome c oxidase subunit VIIa polypeptide 3 (liver);
  • Gene: [14^/ERVT1] endogenous retroviral sequence, truncated 1 (band T1, 26 kb);
  • Gene: [14^/ESAT] esterase activator;
  • Gene: [14^/FDPSL3] farnesyldiphosphate synthetase (dimethylallyltransferase)-like 3; farnesyldiphosphate synthetase (geranyl-trans-transferase)-like 3;
  • Gene: [14^/FTHL13] ferritin, heavy polypeptide-like 13;
  • Gene: [14^/GABRIL4] diazepam binding inhibitor, like 4; [DBIL4 ]
  • Gene: [14^/K12T] temperature sensitivity complementation, K12;
  • Gene: [14^/LAMRL3] laminin receptor-like 3;
  • Gene: [14^/LRE3] LINE retrotransposable element 3;
  • Gene: [14^/M195] external membrane protein (MM 195 kD);
  • Gene: [14^/MSK30] antigen MSK30 (monoclonal antibody A42);
  • Gene: [14^/PPIP2] peptidylprolyl cis-trans-isomerase (cyclophilin) pseudogene 2;
  • Gene: [14^/PRKCL1] protein kinase C-like 1; serine/threonine kinase 3; serine/threonine kinase N; protein kinase C related kinase;
  • Gene: [14^/RNASE4] ribonuclease, RNase A family, 4;
  • Gene: [14^/RNASE6] ribonuclease, RNase A family, 6;
  • Gene: [14^/RPL36A] ribosomal protein L36a (L44); [RPL44 ]
  • Gene: [14^/SIX1] sine oculis homeobox (Drosophila) homolog 1;
  • Gene: [14^/SLC10A1] solute carrier family 10 (sodium/bile acid cotransporter family), member 1; [NTCP ]
  • Gene: [14^/TEP1] telomerase-associated protein 1; telomerase protein component 1 (p80); [TP1 TLP1 ]
  • Gene: [14^/TSE3] tissue specific extinguisher 3;
  • Gene: [14^/UNGP2] uracil-DNA glycosylase pseudogene 2;
  • Gene: [15p111/D15Z1] satellite DNA, unknown class (probe pHSR);
  • Gene: [15p111/D15Z2] satellite DNA, unknown sequence (probe pIR19);
  • Gene: [15p111/D15Z3] satellite DNA, alpha (Chr 15 specific subset; probe pTRA-20);
  • Gene: [15p111/D15Z4] satellite DNA, alpha (Chr 15 specific subset; probe pTRA-25);
  • Gene: [15p12/D15FB2S1] satellite DNA, beta, NOR3-flanking subset 1; [DNFB2S1 ]
  • Gene: [15p12/D15FB2S2] satellite DNA, beta, NOR3-flanking subset 2; [DNFB2S2 ]
  • Gene: [15p12/RNR3BAM] rDNA subset 3, BamHI-RFLP in downstream 28S rRNA gene (30-50 copies); [RNR3 ]
  • Gene: [15p12/RNR3SN1] RNA, ribosomal 3, 8S-1 RNA (sn-PolI; 30-50 copies); [RNR3 SNPIRNA1 ]
  • Gene: [15p12/RNR3SN2] RNA, ribosomal 3, 8S-2 RNA (sn-PolI; 30-50 copies); [RNR3 SNPIRNA2 ]
  • Gene: [15p12/RNR3UA] RNA, ribosomal 3, accessory unit 5.8S rRNA (30-50 copies); [RNR3 ]
  • Gene: [15p12/RNR3UL] RNA, ribosomal 3, large unit 28S rRNA (30-50 copies); [RNR3 ]
  • Gene: [15p12/RNR3US] RNA, ribosomal 3, small unit 18S rRNA (30-50 copies); [RNR3 ]
  • Gene: [15q/ALS5] amyotrophic lateral sclerosis 5;
  • Gene: [15q/BUB1B] budding uninhibited by benzimidazoles 1 (yeast homolog), beta; [BUBR1 ]
  • Gene: [15q/CHR39B] cholesterol repressible protein 39B;
  • Gene: [15q/CPL1] ceruloplasmin-like 1;
  • Gene: [15q/DUT] deoxyuridine 5'-triphosphate nucleotidohydrolase; dUTP pyrophosphatase;
  • Gene: [15q/EYCL3] eye color 3 (brown); brown eye color; total brown iris pigmentation; [BEY2 ]
  • Gene: [15q/FDPSL4] farnesyldiphosphate synthetase (dimethylallyltransferase)-like 4; farnesyldiphosphate synthetase (geranyl-trans-transferase)-like 4;
  • Gene: [15q/HCL3] hair color 3 (brown); brown hair color;
  • Gene: [15q/HCVS] coronavirus 229E sensitivity;
  • Gene: [15q/HDC] histidine decarboxylase;
  • Gene: [15q/ITPKA] inositol 1,4,5-triphosphate (1D-myo-) 3-kinase A;
  • Gene: [15q/MAP1A] microtubule-associated protein 1A; microtubule-associated protein 1-like; [MAP1L ]
  • Gene: [15q/MFAP1] microfibrillar-associated protein 1;
  • Gene: [15q/MIC12] antigen MIC12 (monoclonal antibody 30.2A8);
  • Gene: [15q/MIC7] antigen MIC7 identified by monoclonal antibody 28.3.7;
  • Gene: [15q/MSK15] antigen MSK15 (monoclonal antibody SV13); [SV13 ]
  • Gene: [15q/MSK17] antigen MSK17 (monoclonal antibody F23); [F23 ]
  • Gene: [15q/NEDD4] neural precursor cell expressed, developmentally down-regulated 4;
  • Gene: [15q/NMB] neuromedin B; [F23 ]
  • Gene: [15q/SLC12A1] solute carrier family 12 (sodium/potassium/chloride transporters), member 1; Bartter syndrome, type 1 (hypokalemic alkalosis with hypercalciuria); [NKCC2 ]
  • Gene: [15q/TYRO3P] protein tyrosine kinase TYRO3 pseudogene;
  • Gene: [15q/TYRO3] protein tyrosine kinase TYRO3; protein tyrosine kinase RSE; protein tyrosine kinase SKY; sea-related receptor tyrosine kinase;
  • Gene: [15q1/ACADI] isovaleryl coenzyme A dehydrogenase; isovalericacidemia;
  • Gene: [15q1/ACCPN] agenesis of the corpus callosum with peripheral neuropathy (Charlevoix disease; Andermann syndrome);
  • Gene: [15q1/B2MR] beta-2-microglobulin regulator;
  • Gene: [15q1/BCL8] B-cell chronic lymphatic leukemia 8 (B-CLL: lymphoma 8);
  • Gene: [15q1/EDM4] epiphyseal dysplasia, multiple 4 (with early-onset diabetes mellitus, Wolcott-Rallison syndrome);
  • Gene: [15q1/FMN] formin (homolog of murine limb deformity gene); [LD ]
  • Gene: [15q1/GABRA5] gamma-aminobutyric acid (GABA) A receptor, alpha 5;
  • Gene: [15q1/GABRB3] gamma-aminobutyric acid (GABA) A receptor, beta 3;
  • Gene: [15q1/GABRG3] gamma-aminobutyric acid (GABA) A receptor, gamma 3;
  • Gene: [15q1/IGHDYP1] immunoglobulin heavy chain, diversity pseudogene 1; [IGHDY2 IGD2 ]
  • Gene: [15q1/MANAA] mannosidase, alpha A, cytoplasmic;
  • Gene: [15q1/NDN] necdin (mouse) homolog;
  • Gene: [15q1/OCA2] P protein; albinism, oculocutaneous, II (pink-eye dilution (murine) homolog);
  • Gene: [15q1/PAR1] transcript 1 from Prader-Willi/Angelman region; [D15S227E ]
  • Gene: [15q1/PAR5] transcript 1 from Prader-Willi/Angelman region; [D15S226E ]
  • Gene: [15q1/PWCR] Prader-Willi syndrome chromosome region; [PWS ]
  • Gene: [15q1/RPL5P1] ribosomal protein L5 pseudogene 1;
  • Gene: [15q1/RYR3] ryanodine receptor 3 (brain; calcium release channel);
  • Gene: [15q1/SGNE1] secretory granule neuroendocrine protein 7B2; [7B2 ]
  • Gene: [15q1/SNRPN] small nuclear ribonucleoprotein polypeptide N;
  • Gene: [15q1/UBE3A] ubiquitin protein ligase E3A; human papilloma virus E6-associated protein; Angelman syndrome (AS; happy puppet syndrome; MIM:105830);
  • Gene: [15q1/ZNF127] zinc finger protein 127; [D15S9 ]
  • Gene: [15q111/SPG6] spastic paraplegia 6 (autosomal dominant);
  • Gene: [15q12/IPW] imprinted in Prader-Willi syndrome;
  • Gene: [15q13/TJP1] tight junction protein 1 (zona occludens 1); [ZO1 ]
  • Gene: [15q14/ACTA4] actin, alpha 4, cardiac muscle; cardiomyopathy, idiopathic dilated; [ACTC ]
  • Gene: [15q14/CHRNA7] cholinergic receptor, nicotinic, alpha polypeptide 7 (neuronal);
  • Gene: [15q15/CAPN3] calpain, large polypeptide L3 (catalytic); calcium-activated neutral proteinase (protein p94); limb girdle muscular dystrophy 2A (autosomal recessive; MIM:253600); Leyden-Moebius muscular dystrophy (pelvofemoral; MIM:253
  • Gene: [15q15/CDAN1] congenital dyserythropoietic anemia, type I; [CDAI ]
  • Gene: [15q15/CKMT1] creatine kinase, mitochondrial 1 (ubiquitous);
  • Gene: [15q15/EPB42] erythrocyte membrane protein band 4.2 (pallidin); hereditary hemolytic anemia (alleles 4.2-Lisboa and 4.2-Tuzear); hereditary spherocytosis (Japanese type, autosomal recessive, alleles 4.2-Notame and 4.2-Nippon);
  • Gene: [15q15/GRP58] glucose regulated protein, 58kD; thiol-dependent reductase? GRP58; protein disulfide isomerase (EC:5.3.4.1);
  • Gene: [15q15/LTK] leukocyte tyrosine kinase;
  • Gene: [15q15/THBS1] thrombospondin 1; [TSP1 ]
  • Gene: [15q151/RAD51] RAD51 (S. cerevisiae) homolog (E coli RecA homolog); recombination protein A (E coli RecA homolog, RAD51 homolog); [RECA RAD51A ]
  • Gene: [15q2/ADAM10] a disintegrin and metalloprotease domain 10;
  • Gene: [15q2/ANX2] annexin II (lipocortin II; calpactin I heavy chain); [ANX2L4 LPC2 ]
  • Gene: [15q2/B2M] beta-2-microglobulin; hemodialysis-related amyloidosis (HRA); carpal tunnel syndrome (posthemodialysis);
  • Gene: [15q2/BBS4] Bardet-Biedl syndrome 4;
  • Gene: [15q2/CD24L2] antigen CD24-like 2;
  • Gene: [15q2/CDAN3] congenital dyserythropoietic anemia, type III; [CDAIII ]
  • Gene: [15q2/CLN6] ceroid-lipofuscinosis, neuronal 6, late infantile, variant; [LINCL ]
  • Gene: [15q2/CSK] c-src tyrosine kinase;
  • Gene: [15q2/CTSH] cathepsin H;
  • Gene: [15q2/CYP11A] cytochrome P450, subfamily XIA (cholesterol side chain cleavage); cholesterol monooxygenase (P450/scc, side-chain-cleaving); lipoid adrenal hyperplasia (MIM:201710);
  • Gene: [15q2/CYP1A1] cytochrome P450, subfamily IA (aromatic compound-inducible) polypeptide 1; dioxin-inducible P1-450 (TCDD-inducible; P1-450);
  • Gene: [15q2/CYP1A2] cytochrome P450, subfamily IA (aromatic compound-inducible) polypeptide 2; dioxin-inducible P3-450 (TCDD-inducible; P3-450);
  • Gene: [15q2/DFNB16] deafness, autosomal recessive 16;
  • Gene: [15q2/ETFA] electron-transferring-flavoprotein, alpha polypeptide; glutaricaciduria IIA (ETF-alpha deficiency); ethylmalonic-adipicaciduria (glutaric aciduria IIA); multiple acyl-CoA dehydrogenase deficiency (MADD); [GA2A EMA MADD ]
  • Gene: [15q2/FAH] fumarylacetoacetase (hepatorenal tyrosinemia); tyrosinemia, type I (hepatorenal);
  • Gene: [15q2/GPR1] G protein-coupled receptor 1;
  • Gene: [15q2/HEXA] hexosaminidase A, alpha polypeptide; GM2-gangliosidosis I (Tay-Sachs disease, form b/b1, pseudo-AB);
  • Gene: [15q2/IDH2] isocitrate dehydrogenase 1 (NADP+), mitochondrial;
  • Gene: [15q2/IGF1R] insulin-like growth factor 1 receptor; somatomedin C receptor (IGF1 receptor);
  • Gene: [15q2/ISLR] immunoglobulin superfamily containing leucine-rich repeat;
  • Gene: [15q2/LIPC] lipase, hepatic; hepatic lipase deficiency;
  • Gene: [15q2/LOXL1] lysyl oxidase-like 1;
  • Gene: [15q2/MADH3] MAD (mothers against decapentaplegic, Drosophila) homolog 3; [SMAD3 JV15-2 ]
  • Gene: [15q2/MEIS2] homeobox protein Meis (mouse) homolog 2; [MRG1 ]
  • Gene: [15q2/MPI] mannose phosphate isomerase; carbohydrate-deficient glycoprotein syndrome, type Ib (due to phosphomannose isomerase deficiency; MIM:602579);
  • Gene: [15q2/MYO1C] myosin IC;
  • Gene: [15q2/NEO1] neogenin (chicken) homolog 1; [NGN ]
  • Gene: [15q2/NTRK3] neurotrophic tyrosine kinase, receptor, type 3;
  • Gene: [15q2/PEPN] aminopeptidase N (antigen CD13; p150; alanyl aminopeptidase); glycoprotein p150 (CD13; leukocyte; aminopeptidase N);
  • Gene: [15q2/PHAP1] human HLA class II associated protein 1;
  • Gene: [15q2/PKM] pyruvate kinase, muscle (M1; M2; PK2); pyruvate kinase, kidney (PK3; MIM:179040); thyroid hormone binding protein, cytosolic (p58; MIM:188555);
  • Gene: [15q2/RPL4] ribosomal protein L4;
  • Gene: [15q2/RPLP1] ribosomal protein, large, P1;
  • Gene: [15q2/TRAP1] tumor rejection antigen (gp96) pseudogene 1;
  • Gene: [15q21/MYO5A] myosin VA (heavy polypeptide 12, myoxin); Griscelli disease; [MYH12 ]
  • Gene: [15q21/PRKM6] protein kinase, mitogen-activated 6; MAP kinase 6 (p97); extracellular signal-regulated kinase 3 (ERK3; p97);
  • Gene: [15q21/TCF12] transcription factor 12 (HTF4, helix-loop-helix transcription factor 4);
  • Gene: [15q211/CYP19] cytochrome P450, subfamily XIX (aromatization of androgens); gynecomastia, familial (increased aromatase activity);
  • Gene: [15q211/FBN1] fibrillin 1 (Marfan syndrome); Marfan syndrome 1 (MIM:154700); [FBN MFS1 MFS ]
  • Gene: [15q211/SORD] sorbitol dehydrogenase;
  • Gene: [15q211/WMS] Weill-Marchesani syndrome;
  • Gene: [15q22/CA12] carbonic anhydrase XII;
  • Gene: [15q22/FRA15A] fragile site 15q22, aphidicolin type, common;
  • Gene: [15q22/PML] transcription factor PML (inducer of acute promyelocytic leukemia); promyelocytic leukemia; [MYL APL ]
  • Gene: [15q22/PRKMK1] protein kinase, mitogen-activated, kinase 1 (43.5kD); MAP kinase kinase 1 (MAPKK 1);
  • Gene: [15q22/RORA] RAR-related orphan receptor alpha; [RZRA ]
  • Gene: [15q22/SRP14] signal recognition particle 14kD (homologous Alu RNA-binding protein);
  • Gene: [15q22/TLE3] transducin-like enhancer of split 3, homolog of Drosophila E(spl);
  • Gene: [15q221/TPM1] tropomyosin 1 (skeletal muscle alpha); cardiomyopathy, hypertrophic 3 (MIM:115196); [TMSA CMH3 ]
  • Gene: [15q24/CHRNA3] cholinergic receptor, nicotinic, alpha polypeptide 3 (neuronal); [NACHRA3 ]
  • Gene: [15q24/CHRNA5] cholinergic receptor, nicotinic, alpha polypeptide 5 (neuronal);
  • Gene: [15q24/CHRNB4] cholinergic receptor, nicotinic, beta polypeptide 4 (neuronal);
  • Gene: [15q24/CLK3] CDC-like kinase 3;
  • Gene: [15q24/RABPC1] retinoic acid-binding protein, cellular, 1; [RBP5 CRABP1]
  • Gene: [15q24/RASGRF1] Ras protein-specific guanine nucleotide-releasing factor 1; [GRF1 H-GRF55 ]
  • Gene: [15q25/IDH3A] isocitrate dehydrogenase 1 (NAD+) alpha, mitochondrial;
  • Gene: [15q25/MAN2A2] mannosidase, alpha, class 2A, member 2; mannosidase, alpha type II(X);
  • Gene: [15q25/MFGE8] milk fat globule-EGF factor 8 protein; breast epithelial antigen BA46; [BA46 ]
  • Gene: [15q26/ALDH6] aldehyde dehydrogenase 6;
  • Gene: [15q26/CHD2] chromodomain helicase DNA binding protein 2;
  • Gene: [15q26/CHRM5] cholinergic receptor, muscarinic 5;
  • Gene: [15q26/IDDM3] insulin-dependent diabetes mellitus 3;
  • Gene: [15q26/MEF2A] MADS box transcription enhancer factor 2, polypeptide A; myocyte-specific enhancer factor 2A; [RSRFC4 RSRFC9 ]
  • Gene: [15q26/PCSK6] proprotein convertase subtilisin/kexin type 6; paired basic amino acid cleaving system 4;
  • Gene: [15q26/PRKXP1] protein kinase, X-linked, pseudogene 1;
  • Gene: [15q26/RLBP1] retinaldehyde-binding protein 1; cellular retinaldehyde-binding protein (CRALBP); retinitis pigmentosa, autosomal recessive; [CRALBP ]
  • Gene: [15q26/TFCOUP2] transcription factor COUP 2 (chicken ovalbumin upstream promoter 2); apolipoprotein regulatory protein 1; [ARP1 ]
  • Gene: [15q261/BLM] Bloom's syndrome protein; Bloom syndrome;
  • Gene: [15q261/CSPG1] chondroitin sulfate proteoglycan 1; aggrecan 1 (large aggregating proteoglycan); chondroitin sulfate proteoglycan (melanoma-associated; MCSP); antigen MSK16 (monoclonal antibody AO122); [AGC1 MSK16 ]
  • Gene: [15q261/FES] protooncogene tyrosine protein kinase FES/FPS; feline sarcoma (Snyder-Theilen) viral homolog; Fujinami avian sarcoma (PRCII) viral (v-fps) oncogene homolog;
  • Gene: [15q261/PCSK3] proprotein convertase subtilisin/kexin type 3; furin, membrane associated receptor protein; paired basic amino acid cleaving enzyme;
  • Gene: [15^/APBA2] amyloid beta (A4) precursor protein-binding, family A, member 2 (X11-like);
  • Gene: [15^/BCL2A1] BCL2-related protein A1 (BFL1; hematopoietic); [HBPA1 BFL1 ]
  • Gene: [15^/BNC] basonuclin (keratinocyte zinc finger protein);
  • Gene: [15^/COL1AR] collagen, type I, alpha, receptor;
  • Gene: [15^/EEF1B1] eukaryotic translation elongation factor 1 beta 1;
  • Gene: [15^/FGF7] fibroblast growth factor 7 (keratinocyte growth factor; KGF); [KGF HBGF7 ]
  • Gene: [15^/GALK2] galactokinase 2;
  • Gene: [15^/GANC] glucosidase, alpha; neutral C;
  • Gene: [15^/GAPDL6] glyceraldehyde-3-phosphate dehydrogenase-like 6;
  • Gene: [15^/HSPCP2] heat shock 90kD protein pseudogene 2;
  • Gene: [15^/IGKVP2] immunoglobulin kappa polypeptide pseudogene 2;
  • Gene: [15^/IREB2] iron-responsive element binding protein 2;
  • Gene: [15^/MADH6] MAD (mothers against decapentaplegic, Drosophila) homolog 6; [SMAD6 ]
  • Gene: [15^/NF1P1] neurofibromin 1 pseudogene 1;
  • Gene: [15^/PPIB] peptidylprolyl cis-trans-isomerase B (cyclophilin B);
  • Gene: [15^/PYHG11] protein spot in 2-D gels (MM 74 kD);
  • Gene: [15^/PYHG20] protein spot in 2-D gels (MM 10 kD);
  • Gene: [16p1/CA5P] carbonic anhydrase V pseudogene;
  • Gene: [16p1/COX6A2] cytochrome c oxidase subunit VIa polypeptide 2 (heart- and striated muscle-specific isoform);
  • Gene: [16p1/GTF3C1] general transcription factor IIIC, polypeptide 1 (alpha subunit);
  • Gene: [16p1/ICCA] infantile convulsions and paroxysmal choreoathetosis; [FICCA ]
  • Gene: [16p1/PLA2G10] phospholipase A2, group X;
  • Gene: [16p1/PPP4C] protein phosphatase 4 (formerly X), catalytic subunit;
  • Gene: [16p1/RBBP6] retinoblastoma-binding protein 6;
  • Gene: [16p1/RPS15A] ribosomal protein S15a;
  • Gene: [16p1/SULT1A1] sulfotransferase family 1A, phenol-preferring, member 1; sulfotransferase, phenol-preferring 1;
  • Gene: [16p1/SULT1A2] sulfotransferase family 1A, phenol-preferring, member 2; sulfotransferase, phenol-preferring 2;
  • Gene: [16p1/SULT1A3] sulfotransferase family 1A, phenol-preferring, member 3; sulfotransferase, monoamine-preferring;
  • Gene: [16p1/ZNF75A] zinc finger protein 75A;
  • Gene: [16p11/ZNF44] zinc finger protein 44 (KOX 7); [KOX7 ]
  • Gene: [16p11/ZNF48] zinc finger protein 48;
  • Gene: [16p112/ADCY7] adenylate cyclase 7;
  • Gene: [16p112/CD19] antigen CD19 (monoclonal antibody Leu12);
  • Gene: [16p112/EFTU] translational elongation factor Tu, mitochondrial; antigen p43, mitochondrial elongation factor-like protein; [P43 TUFM ]
  • Gene: [16p112/FUS] fusion protein, derived from t(12;16) malignant liposarcoma;
  • Gene: [16p112/ITGAD] integrin, alpha D (antigen CD11D);
  • Gene: [16p112/ITGAM] integrin, alpha M (Mac-1a; CD11B; p170); complement component receptor 3, alpha (p170; antigen CD11B); antigen CD11B (macrophage antigen Mac-1-alpha subunit); [CR3A CD11B ]
  • Gene: [16p112/PHKG2] phosphorylase kinase, gamma 2 (testis/liver); glycogenosis, hepatic (phosphorylase kinase deficiency); cirrhosis due to liver phosphorylase kinase deficiency;
  • Gene: [16p112/PPP2CBP] protein phosphatase 2 (formerly 2A), catalytic subunit, beta isoform pseudogene;
  • Gene: [16p112/PRKM3] protein kinase, mitogen-activated 3; MAP kinase 3 (p44); extracellular signal-regulated kinase 1 (p44);
  • Gene: [16p112/PRSS8] protease, serine, 8 (prostasin);
  • Gene: [16p112/SLC5A2] solute carrier family 5 (sodium/glucose transporter), member 2 (renal); renal glycosuria? (MIM:233100); [SGLT2 ]
  • Gene: [16p112/SLC6A10] solute carrier family 6 (neurotransmitter transporter, creatine, testis-specific), member 10; creatine transporter gene, autosomal;
  • Gene: [16p112/SPN] sialophorin (leukosialin; protein gpL115); antigen CD43 (leukocyte sialoglycoprotein); [GPL115 CD43 ]
  • Gene: [16p112/STX1B] syntaxin 1B;
  • Gene: [16p112/ZNF65] zinc finger protein 65;
  • Gene: [16p12/RP22] retinitis pigmentosa 22 (autosomal recessive);
  • Gene: [16p12/SCNN1B] sodium channel, nonvoltage-gated 1 beta; pseudohypoaldosteronism, type I (autosomal dominant; SCNN1A deficiency; MIM:177735); pseudohypoaldosteronism, type I (autosomal recessive; persian-jewish type; SCNN1B deficiency;
  • Gene: [16p12/SCNN1G] sodium channel, nonvoltage-gated 1 gamma; pseudohypoaldosteronism, type I (autosomal recessive; persian-jewish type; SCNN1G deficiency; MIM:264350); pseudoaldosteronism (Liddle syndrome; SCNN1G deficiency; MIM:177200);
  • Gene: [16p121/ATP2A1] ATPase, Ca++ transporting, cardiac muscle, fast twitch 1; sarcoplasmic reticulum Ca(2+)-ATPase 1; Brody's disease (muscle contracture due to exercise; MIM:601003);
  • Gene: [16p121/CLN3] ceroid-lipofuscinosis, neuronal 3 (juvenile amaurotic family idiocy); Batten disease (neuronal ceroid-lipofuscinosis); juvenile amaurotic family idiocy (Vogt-Spielmeyer/Sjogren disease); [BTS NCL ]
  • Gene: [16p121/FRA16E] fragile site 16p12.1, folic acid type, rare;
  • Gene: [16p121/IL4R] interleukin 4 receptor (antigen CD124);
  • Gene: [16p121/ITGAX] integrin, alpha X (CD11C; p150,95-alpha); antigen CD11C (alpha X integrin; LeuM5); [CD11C LEUM5 ]
  • Gene: [16p123/CDR2] cerebellar degeneration-related autoantigen 2 (62kD);
  • Gene: [16p123/ITGAL] integrin, alpha L (antigen CD11A; p180; LFA1-alpha); antigen CD11A (p180; alpha L integrin); lymphocyte function-associated antigen 1, alpha subunit; [LFA1A CD11A ]
  • Gene: [16p123/PRKCB] protein kinase C, beta polypeptide;
  • Gene: [16p123/UQCRC2] ubiquinol-cytochrome c reductase core protein 2;
  • Gene: [16p13/CLCN7] chloride channel 7;
  • Gene: [16p13/GFER] growth factor, erv1 (S. cerevisiae)-like (augmenter of liver regeneration);
  • Gene: [16p13/GRIN2A] glutamate receptor, ionotropic, N-methyl-D-aspartate 2A; [NMDAR2A ]
  • Gene: [16p13/PMM2] phosphomannomutase 2; carbohydrate-deficient glycoprotein syndrome, type Ia (Jaeken syndrome; MIM:212065);
  • Gene: [16p13/PPL] periplakin;
  • Gene: [16p131/MRP] multiple drug resistance-associated protein;
  • Gene: [16p131/MYH11] myosin, heavy polypeptide 11, smooth muscle;
  • Gene: [16p131/PXE] pseudoxanthoma elasticum (MIM:264800);
  • Gene: [16p1311/CRYM] crystallin, mu polypeptide;
  • Gene: [16p1311/FRA16A] fragile site 16p13.11, folic acid type, rare;
  • Gene: [16p1311/PDE1B] phosphodiesterase 1B, calcium/calmodulin-dependent (63kD);
  • Gene: [16p1311/SAH] SA (rat hypertension-associated) homolog; [SA ]
  • Gene: [16p1311/UMOD] uromodulin (uromucoid, Tamm-Horsfall glycoprotein);
  • Gene: [16p1313/ERCC4] excision repair cross-complementing rodent repair deficiency, complementation group 4; xeroderma pigmentosum, complementation group F (MIM:278760); [XPF ]
  • Gene: [16p1313/GSPT1] G1 to S phase transition 1;